Canonical Allele Identifier: PA2825084071
Gene: CFI HGNC NCBI

Linked Data

ClinVar Variation Id: 3235979
ClinVar RCV Id: RCV004555240

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000195.3:p.Asp524Gly
CA357854665
NM_000204.5:c.1571A>G